| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7438182-7438326 | Rare:32 | ||||
| chr17:7455539-7455840 | Common:3; Rare:82; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:7479490-7479740 | Common:1; Rare:44 | ||||
| chr17:7484214-7484391 | Common:2; Rare:77 | ||||
| chr17:7484611-7484848 | Common:1; Rare:97 | ||||
| chr17:7549635-7549638 | |||||
| chr17:7558555-7558753 | Rare:43 | ||||
| chr17:7561784-7561996 | Common:2; Rare:58 | ||||
| chr17:7576106-7576132 | Rare:4 | ||||
| chr17:7583501-7583865 | Common:1; Rare:146; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:7584063-7584250 | Rare:46 | ||||
| chr17:7674859-7675230 | Common:1; Rare:109; Clinvar:35; Clinvar (benign):30; Clinvar (pathogenic):23 | ||||
| chr17:7686476-7686677 | Rare:51 | ||||
| chr17:7687376-7687419 | Rare:5; Clinvar:1 | ||||
| chr17:7843673-7843740 | Rare:23 |